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作 者:路淑淑 李文馨 张贝贝 李智强[2] 靳英辉 侯宁 LU Shushu;LI Wenxin;ZHANG Beibei;LI Zhiqiang;JIN Yinghui;HOU Ning(School of Pharmacy,Shandong University,Jinan 250012,China;Shandong Mental Health Center,Jinan 250013,China;Shandong Institute for Food and Drug Control,Jinan 250101,China;Center for Evidence-based Nursing,Tianjin University of TCM,Tianjin 300193,China;Center for Evidence-based Medicine and TranslationalMedicine,Zhongnan Hospital of Wuhan University,Wuhan 430071,China;Dept. of Pharmacy,ShandongProvincial Hospital Affiliated to Shandong University,Jinan 250021,China)
机构地区:[1]山东大学药学院,济南250012 [2]山东省精神卫生中心,济南250013 [3]山东省食品药品检验研究院,济南250101 [4]天津中医药大学循证护理中心,天津300193 [5]武汉大学中南医院循证与转化医学中心,武汉430071 [6]山东大学附属省立医院药学部,济南250021
出 处:《中国药房》2018年第10期1395-1400,共6页China Pharmacy
基 金:国家自然科学基金资助项目(No.81603496)
摘 要:目的:系统评价艾司西酞普兰与度洛西汀治疗抑郁症的有效性和安全性,为临床治疗提供循证参考。方法:计算机检索Pub Med、万方数据库、中文科技数据库、中国期刊全文数据库、中国生物医学文献数据库,收集艾司西酞普兰(试验组)与度洛西汀(对照组)治疗抑郁症的临床随机对照试验(RCT),提取数据并按照Cochrane系统评价员手册5.3推荐的偏倚风险评估工具评价文献质量后,采用Rev Man 5.3软件对数据进行Meta分析。结果:共纳入25项RCT,合计2 621例患者。Meta分析结果显示,两组患者治疗第1、2、4、6、8周的总有效率及治疗第4、6、8周的治愈率比较,差异均无统计学意义(P>0.05)。两组女性患者总有效率[RR=0.96,95%CI(0.88,1.05),P=0.42]、女性患者治愈率[RR=0.91,95%CI(0.78,1.06),P=0.24]、老年患者总有效率[RR=0.96,95%CI(0.84,1.11),P=0.61]、老年患者治愈率[RR=0.90,95%CI(0.54,1.49),P=0.69]比较,差异均无统计学意义。试验组患者便秘[RR=0.59,95%CI(0.42,0.81),P=0.001]、口干[RR=0.65,95%CI(0.51,0.82),P=0.000 4]、恶心[RR=0.68,95%CI(0.56,0.83),P=0.000 2]、食欲降低[RR=0.74,95%CI(0.55,0.99),P=0.04]的发生率均显著低于对照组,差异均有统计学意义。结论:艾司西酞普兰与度洛西汀治疗抑郁症的有效性相当,但在安全性方面艾司西酞普兰更优。OBJECTIVE: To systematically evaluate the effectiveness and safety of escitalopram and duloxetine in the treatment of depression, and provide evidence-based reference for clinical treatment. METHODS: Retrieved from Pub Med,Wanfang database,VIP,CNKI and CBM,randomized controlled trials(RCTs) about escitalopram(trial group) and duloxetine(control group)in the treatment of depression were collected. Meta-analysis was conducted by using Rev Man 5.3 software after data extraction and quality evaluation according to bias risk assessment tool recommended by system evaluator manual 5.3.RESULTS:Finally 25 RCTs were included,involving 2 621 patients. The results of Meta-analysis showed that there was no statistical significance in total response rate between 2 groups after 1,2,4,6,8 weeks of treatment or cure rate between 2 groups after 4,6,8 weeks of treatment(P0.05). There was no statistical significance in total response rate [RR=0.96,95%CI(0.88,1.05),P=0.42] or cure rate [RR=0.91,95%CI(0.78,1.06),P=0.24] of female patients,as well as total response rate [RR=0.96,95%CI(0.84,1.11),P=0.61] or cure rate [RR=0.90,95%CI(0.54,1.49),P=0.69] of elderly patients between 2 groups. The incidence of constipation [RR=0.59,95%CI(0.42,0.81),P=0.001],dry mouth [RR=0.65,95%CI(0.51,0.82),P=0.000 4],nausea [RR=0.68,95% CI(0.56,0.83),P=0.000 2] and decreased appetite [RR=0.74,95% CI(0.55,0.99),P=0.04] in trial group were significantly lower than control group,with statistical significance. CONCLUSIONS:The effectiveness of escitalopram is similar to duloxetine in the treatment of depression,but the safety of escitalopram is better than duloxetine.
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